Colon Cancer: Gene >> KCNF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10912697:10912697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>A
AA Mutation	p.Glu91Lys(p.E91K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10913651:10913651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225T>G
AA Mutation	p.Phe409Val(p.F409V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10912569:10912569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143G>A
AA Mutation	p.Arg48Gln(p.R48Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10912859:10912859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764108317
CDS Mutation	c.433G>A
AA Mutation	p.Val145Met(p.V145M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10913145:10913145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719G>A
AA Mutation	p.Arg240His(p.R240H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10913127:10913127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701C>T
AA Mutation	p.Thr234Ile(p.T234I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10913676:10913676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250G>A
AA Mutation	p.Arg417His(p.R417H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10912980:10912980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.554C>T
AA Mutation	p.Ala185Val(p.A185V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10913109:10913109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683C>T
AA Mutation	p.Ala228Val(p.A228V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295082
Start	10913176:10913176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295082
Start	10913350:10913350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295082
Start	10912831:10912831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766200572
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295082
Start	10913299:10913299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295082
Start	10912885:10912885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295082
Start	10912538:10912538(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.115delG
AA Mutation	p.Asp39ThrfsTer62(p.D39Tfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000295082
Start	10912526:10912526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100C>T
AA Mutation	p.Gln34Ter(p.Q34*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295082
Start	10912512:10912513(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.92dupG
AA Mutation	p.Val32ArgfsTer15(p.V32Rfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KCNF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295082
Start	10913195:10913195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.769A>G
AA Mutation	p.Ile257Val(p.I257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295082
Start	10913875:10913875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1449G>A
Mutation Classification	Silent
Feature Type	Transcript